Examlex
The "Bridge to Nowhere"
Chromosome 15
One of the 23 pairs of human chromosomes, carrying genes that can be involved in various genetic disorders and characteristics.
Fragile X Syndrome
A human genetic disorder caused by a fragile site that occurs near the tip on the X chromosome; effects range from mild learning disabilities to severe intellectual disability and hyperactivity.
CGG Sequences
Specific sequences of DNA nucleotides comprising cytosine and guanine, often studied for their role in genetic diseases.
Genomic Imprinting
A biological occurrence where specific genes are manifested based on which parent they are inherited from.
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